Department of Emergency Medicine, Johns Hopkins University, Baltimore, MD, USA.
Diagn Microbiol Infect Dis. 2012 Sep;74(1):22-7. doi: 10.1016/j.diagmicrobio.2012.05.015. Epub 2012 Jul 17.
This study aimed to conduct a pilot evaluation of broad-based multiprobe polymerase chain reaction (PCR) in clinical cerebrospinal fluid (CSF) samples compared to local conventional PCR/culture methods used for bacterial meningitis surveillance. A previously described PCR consisting of initial broad-based detection of Eubacteriales by a universal probe, followed by Gram typing, and pathogen-specific probes was designed targeting variable regions of the 16S rRNA gene. The diagnostic performance of the 16S rRNA assay in ""127 CSF samples was evaluated in samples from patients from Togo, Africa, by comparison to conventional PCR/culture methods. Our probes detected Neisseria meningitidis, Streptococcus pneumoniae, and Haemophilus influenzae. Uniprobe sensitivity and specificity versus conventional PCR were 100% and 54.6%, respectively. Sensitivity and specificity of uniprobe versus culture methods were 96.5% and 52.5%, respectively. Gram-typing probes correctly typed 98.8% (82/83) and pathogen-specific probes identified 96.4% (80/83) of the positives. This broad-based PCR algorithm successfully detected and provided species level information for multiple bacterial meningitis agents in clinical samples.
本研究旨在对临床脑脊液 (CSF) 样本进行基于广泛探针的多重聚合酶链反应 (PCR) 的初步评估,与用于细菌性脑膜炎监测的当地常规 PCR/培养方法进行比较。设计了一种先前描述的 PCR,由通用探针进行的 Eubacteriales 的初始广泛检测、革兰氏分型和针对 16S rRNA 基因可变区的病原体特异性探针组成。通过与常规 PCR/培养方法比较,在来自非洲多哥的患者的 127 份 CSF 样本中评估了 16S rRNA 检测方法的诊断性能。我们的探针检测到脑膜炎奈瑟菌、肺炎链球菌和流感嗜血杆菌。与常规 PCR 相比,单探针的敏感性和特异性分别为 100%和 54.6%。单探针与培养方法的敏感性和特异性分别为 96.5%和 52.5%。革兰氏分型探针正确分型了 98.8%(82/83)的阳性样本,病原体特异性探针鉴定了 96.4%(80/83)的阳性样本。这种基于广泛探针的 PCR 算法成功地在临床样本中检测到多种细菌性脑膜炎病原体,并提供了种水平的信息。